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Spastin and atlastin, two proteins mutated in autosomal dominant hereditary spastic paraplegia, are binding partners
The pure hereditary spastic paraplegias (HSPs) are a group of conditions in which there is progressive length-dependent degeneration of the distal ends of the corticospinal tract axons, resulting in spastic paralysis of the legs. Pure HSPs are most frequently inherited in an autosomal dominant patte...
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| Autores principales: | , , , , , , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
2005
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2443951/ https://ncbi.nlm.nih.gov/pubmed/16339213 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddi447 |
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